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Clinical Research Coordinator

Job in Tyler, Smith County, Texas, 75701, USA
Listing for: Medix™
Full Time position
Listed on 2026-01-12
Job specializations:
  • Healthcare
    Clinical Research
Salary/Wage Range or Industry Benchmark: 28 - 35 USD Hourly USD 28.00 35.00 HOUR
Job Description & How to Apply Below
Position: Clinical Research Coordinator 247118

This range is provided by Medix™. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$28.00/hr - $35.00/hr

Direct message the job poster from Medix™

Schedule: Monday – Thursday, 8:00 AM – 5:00 PM; occasional Fridays. Flexibility required as the study pipeline grows.

Primary Site: 2737 S. Broadway, Tyler, TX 75701 (occasional travel to nearby hospital)

Overview:

We are seeking a highly motivated Clinical Research Coordinator (CRC) with strong patient-facing experience to support clinical trial operations at a busy research site in Tyler, TX. This is a hands-on role requiring initiative, clinical research expertise, and the ability to work independently alongside a fast-paced Principal Investigator.

Key Responsibilities:
  • Engage directly with patients for clinical trial activities
  • Screen and enroll participants according to protocol-defined inclusion/exclusion criteria
  • Thoroughly review and interpret clinical trial protocols
  • Collect, document, and manage clinical trial data with a high level of accuracy
  • Conduct registry trial assessments, including review and documentation of patient pain scales
  • Collaborate with the Principal Investigator to ensure studies remain on track
Preferred Experience:
  • Previous experience in patient recruitment
  • Background in orthopedic or device trials
  • Familiarity with device/implant studies for back and knee
  • Experience with registry trials involving long-term follow-up
  • Back and knee implant/device trials
  • Ongoing registry studies requiring annual patient visits and assessments
  • Restorative and knee-focused clinical trials
Required Qualifications:
  • Hands-on experience as a Clinical Research Coordinator
  • Strong understanding of clinical trial protocols and processes
  • Proven ability to work independently and take initiative
  • Comfortable in a fast-paced environment with minimal oversight
  • Excellent documentation and data management skills
Ideal Candidate Attributes:
  • Independent, confident, and proactive
  • Quick-thinking and fast learner
  • Strong communication and organizational skills
  • Capable of managing a dynamic workload with minimal supervision
Seniority level

Associate

Employment type

Full-time

Job function

Research

Industries

Hospitals and Health Care

Referrals increase your chances of interviewing at Medix™ by 2x

Inferred from the description for this job

Medical insurance

Vision insurance

401(k)

Disability insurance

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